Evidence map›Paper›PMID 26343849›Full record

ArticleVaccines2013

A Modified Bacillus Calmette-Guérin (BCG) Vaccine with Reduced Activity of Antioxidants and Glutamine Synthetase Exhibits Enhanced Protection of Mice despite Diminished in Vivo Persistence.

Carolyn M Shoen, Michelle S DeStefano, Cynthia C Hager, Kyi-Toe Tham, Miriam Braunstein, Alexandria D Allen, Hiriam O Gates, Michael H Cynamon, Douglas S Kernodle

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Carolyn M ShoenVeterans Affairs Medical Center, Syracuse, NY 13212, USA. shoenc@cnyrc.org.
Michelle S DeStefanoVeterans Affairs Medical Center, Syracuse, NY 13212, USA. Michelle.Destefano@va.gov.
Cynthia C HagerDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA. cindy.hager@vanderbilt.edu.
Kyi-Toe ThamDepartment of Pathology, Vanderbilt University Medical Center, Nashville, TN 37232, USA. kyitoe@catham.org.
Miriam BraunsteinDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC 27599, USA. braunste@med.unc.edu.
Alexandria D AllenDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA. Alexandria.Allen@mlh.org.
Hiriam O GatesDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA. hirham@bellsouth.net.
Michael H CynamonVeterans Affairs Medical Center, Syracuse, NY 13212, USA. Michael.Cynamon@va.gov.
Douglas S KernodleDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA. doug.kernodle@vanderbilt.edu.
Vanderbilt University Medical Center · USUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Early attempts to improve BCG have focused on increasing the expression of prominent antigens and adding recombinant toxins or cytokines to influence antigen presentation. One such modified BCG vaccine candidate has been withdrawn from human clinical trials due to adverse effects. BCG was derived from virulent Mycobacterium bovis and retains much of its capacity for suppressing host immune responses. Accordingly, we have used a different strategy for improving BCG based on reducing its immune suppressive capacity. We made four modifications to BCG Tice to produce 4dBCG and compared it to the parent vaccine in C57Bl/6 mice. The modifications included elimination of the oxidative stress sigma factor SigH, elimination of the SecA2 secretion channel, and reductions in the activity of iron co-factored superoxide dismutase and glutamine synthetase. After IV inoculation of 4dBCG, 95% of vaccine bacilli were eradicated from the spleens of mice within 60 days whereas the titer of BCG Tice was not significantly reduced. Subcutaneous vaccination with 4dBCG produced greater protection than vaccination with BCG against dissemination of an aerosolized challenge of M. tuberculosis to the spleen at 8 weeks post-challenge. At this time, 4dBCG-vaccinated mice also exhibited altered lung histopathology compared to BCG-vaccinated mice and control mice with less well-developed lymphohistiocytic nodules in the lung parenchyma. At 26 weeks post-challenge, 4dBCG-vaccinated mice but not BCG-vaccinated mice had significantly fewer challenge bacilli in the lungs than control mice. In conclusion, despite reduced persistence in mice a modified BCG vaccine with diminished antioxidants and glutamine synthetase is superior to the parent vaccine in conferring protection against M. tuberculosis. The targeting of multiple immune suppressive factors produced by BCG is a promising strategy for simultaneously improving vaccine safety and effectiveness.

Indexed as

antioxidantsBacillus Calmette-Guérin (BCG)glutamine synthetaseimmune suppressionimmunitysigma factorsuperoxide dismutasetuberculosisvaccine

Identifiers

PMID26343849
PMCPMC4552197
OpenAlexW2031580970

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.